A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416986



Internal ID21074539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143508801..143515500hg38UCSC Ensembl
chr7:143205894..143212593hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233102
Samples
Known GenesEPHA1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416986
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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